Allele-specific amplification

ABSTRACT

The present invention includes a method of allele-specific amplification, utilizing an allele-specific oligonucleotide, at least partially complementary to more than one variant of the target sequence, but having a 3′-terminal nucleotide complementary to only one variant of the target sequence and having at least one nucleotide with a base covalently modified at the exocyclic amino group, wherein the allele-specific oligonucleotide is extended by a nucleotide-incorporating biocatalyst predominantly when hybridized to the variant of the target sequence for which it has said complementary 3′-terminal nucleotide.

CROSS-REFERENCE TO RELATED APPLICATION

The present application claims the benefit of provisional applicationNo. 61/106,783 filed Oct. 20, 2008, the content of which is herebyincorporated herein by reference in its entirety.

SEQUENCE LISTING

This application is a divisional of U.S. application Ser. No. 12/582,068filed on Oct. 20, 2009, which claims the benefit of U.S. ProvisionalApplication Ser. No. 61/106,783 filed Oct. 20, 2008. Each of thesespecifications are hereby incorporated by reference in their entirety.

FIELD OF THE INVENTION

The invention relates to the field of nucleic acid amplification andspecifically, to the field of allele-specific amplification.

BACKGROUND OF THE INVENTION

Allele-specific amplification of nucleic acids allows for simultaneousamplification and analysis of the target sequence. Allele-specificamplification is commonly used when the target nucleic acid is suspectedof having one or more subpopulations with a variation (polymorphism) inits sequence. DNA polymorphisms are used in DNA profile analysis(forensics, paternity testing, tissue typing for organ transplants),genetic mapping, as well as detection of rare mutations, such as thoseoccurring in cancer cells in the background of cells with normal DNA.

In a successful allele-specific amplification, the desired variant ofthe target nucleic acid is amplified, while the other variants are not,at least not to a detectable level. A typical allele-specificamplification assay involves a polymerase chain reaction (PCR) where atleast one primer is complementary to the region with a suspectedpolymorphism. The design of the allele-specific primer is such thatprimer extension occurs only when a certain variant of the polymorphismis present. In its simplest form, the allele-specific primer has a3′-terminal nucleotide complementary to the desired variant of thepolymorphic nucleotide in the target. Often a single mismatch at the3′-terminus of the primer is sufficient to preclude amplification of theundesired variants of the target sequence. However, specificity ofamplification varies greatly among different 3′-terminal sequences: somemismatches effectively block extension by the polymerase, while othersdo not, see U.S. Pat. No. 5,639,611.

The success of allelic discrimination depends on the inability of theDNA polymerase to extend mismatched primers. This inability of the DNApolymerase may be modulated by adjusting the reaction conditions toachieve maximum selectivity. Nevertheless, poor selectivity ofallele-specific PCR remains a problem for many polymorphic sequences.

One approach to increasing specificity involves engineeringamplification primers with an internal mismatched nucleotide ornucleotides. This approach proved successful in some systems, see U.S.Pat. No. 5,137,806.

Another approach to increasing specificity involves chemicalmodification of the primers. For example, it was found that certain 2′-Cand 4′-C modifications of the deoxyribose of some nucleotides in theprimer enhance allele discrimination by the polymerase. See Gaster, J.and Marx, A., Chem. Eur. J. 2005, 11:1861-1870. In another study, it wasfound that allelic discrimination is enhanced by the use of an unnaturalpyrimidine base in one of the nucleotides in the primer, specifically,pseudoisocytidine with various substituents in the 6-position of thepyrimidine ring, see U.S. Pat. No. 7,408,051.

In the context of real-time allele-specific PCR, the selectivity of theassay may be measured as the difference in the threshold cycle number(Ct) between the matched and mismatched templates. A greater differenceindicates a greater delay in amplification of the mismatched templateand thus a greater discrimination between alleles. The modifieddeoxyribose has been shown to result in Ct differences of between 1 and14 cycles. The use of pseudoisocytidine resulted in a 7-cycle delay inamplification of the mismatched template. This degree of discriminationis insufficient for many applications, where the sample contains severalvariants of the template, all competing for amplification. Often themismatched template is present in much greater amounts than the matchedtemplate. For example, in tissue samples, only a small fraction of cellsmay be malignant and carry the mutation (“matched template”), targetedby the allele-specific amplification assay. The template present innormal cells may be amplified less efficiently, but the overwhelmingnumbers of normal cells will overcome any delay in amplification anderase any advantage of the mutant template. To detect rare mutations inthe presence of the wild-type template, the specificity of theallele-specific amplification assay needs to be improved.

SUMMARY OF THE INVENTION

In a first aspect, the invention relates to an improved method ofallele-specific amplification, wherein one or more nucleotides in theallele-specific primer or primers are modified by a covalent linkage ofa modifier group to an exocyclic amino group of the nucleobase. Themodification may occur internally or at the 3′-end of the primer, orboth.

In a second aspect, the invention relates to a method of allele-specificamplification of a variant of a target sequence, which exists in theform of several variant sequences, comprising

-   -   (a) providing a sample, possibly containing at least one variant        of a target sequence;    -   (b) providing a first oligonucleotide, at least partially        complementary to one or more variants of the target sequence;    -   (c) providing a second oligonucleotide, at least partially        complementary to one or more variants of the target sequence,        having at least one 3′-terminal nucleotide complementary to only        one variant of the target sequence; wherein said second        oligonucleotide incorporates at least one nucleotide with a base        covalently modified at the exocyclic amino group;    -   (d) providing conditions suitable for the hybridization of said        first and second oligonucleotides to at least one variant of the        target sequence; and    -   (e) providing conditions suitable for the second oligonucleotide        extension by a nucleotide-incorporating biocatalyst; wherein        said biocatalyst is capable of extending said second        oligonucleotide when it is hybridized to the variant of the        target sequence for which it has said complementary 3′-terminal        nucleotide, and substantially less when said second        oligonucleotide is hybridized to the variant of the target        sequence for which it has a non-complementary 3′-terminal        nucleotide.

In a third aspect, the invention relates to a method of detecting avariant of a target sequence in a sample, which exists in the form ofseveral variant sequences comprising

-   -   (a) hybridizing a first and second oligonucleotides to at least        one variant of the target sequence; wherein the first        oligonucleotide is at least partially complementary to one or        more variant of the target sequence and the second        oligonucleotide is at least partially complementary to one or        more variant of the target sequence and has a 3′-terminal        nucleotide complementary to only one variant of the target        sequence, said second oligonucleotide incorporating at least one        nucleotide with a base covalently modified at the exocyclic        amino group;    -   (b) extending the second oligonucleotide with a        nucleotide-incorporating biocatalyst; wherein said biocatalyst        is capable of detectably extending only the oligonucleotide,        hybridized to the variant of the target sequence for which it        has said complementary 3′-terminal nucleotide; and    -   (c) detecting the products of said second oligonuclotide        extension, wherein the extension signifies the presence of the        variant of a target sequence to which the oligonucleotide has a        complementary 3′-terminal nucleotide.

In a fourth aspect, the invention relates to a kit for allele-specificamplification of a target sequence, which exists in the form of severalvariant sequences, comprising

-   -   (a) a first oligonucleotide, at least partially complementary to        one or more variant of the target sequence; and    -   (b) a second oligonucleotide, at least partially complementary        to one or more variant of the target sequence and having a        3′-terminal nucleotide complementary to only one variant of the        target sequence; wherein said second oligonucleotide        incorporates at least one nucleotide with a base covalently        modified at the exocyclic amino group.

In a fifth aspect, the invention relates to an oligonucleotide forperforming an allele-specific amplification of a target sequence, whichexists in the form of several variant sequences, comprising

-   -   a sequence at least partially complementary to a portion of one        or more variants of said target sequence;    -   a 3′-terminal nucleotide which is complementary to only one        variant of said target sequence and    -   at least one nucleotide with a base covalently modified at the        exocyclic amino group.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a schematic diagram of the allele-specific amplification assayof the present invention.

FIG. 2 shows the results of allele-specific amplification using primerswith internal base modifications.

FIG. 3 shows the results of allele-specific amplification using primerswith one or more internal and 3′-terminal base modifications.

FIG. 4 shows the results of allele-specific amplification using a primerwith a base modification and various DNA polymerases.

FIG. 5 shows the results of allele-specific amplification usingbase-modified primers in the presence of excess amounts of mismatchedtemplate.

FIG. 6 shows an example of a scorpion or scorpion-like probe-primerformat within the meaning of the invention.

FIG. 7 shows a schematic representation of the structure of a scorpionARMS format that can be used according to the invention.

DETAILED DESCRIPTION OF THE INVENTION Definitions

Unless defined otherwise, all technical and scientific terms used hereinhave the same meaning as commonly understood by one of ordinary skill inthe art to which this invention pertains. In describing and claiming thepresent invention, the following definitions will be used.

The term “nucleic acid” refers to polymers of nucleotides (e.g.,ribonucleotides, deoxyribonucleotides, nucleotide analogs etc.) andcomprising deoxyribonucleic acids (DNA), ribonucleic acids (RNA),DNA-RNA hybrids, oligonucleotides, polynucleotides, aptamers, peptidenucleic acids (PNAs), PNA-DNA conjugates, PNA-RNA conjugates, etc., thatcomprise nucleotides covalently linked together, either in a linear orbranched fashion. A nucleic acid is typically single-stranded ordouble-stranded and will generally contain phosphodiester bonds,although in some cases, nucleic acid analogs are included that may havealternate backbones, including, for example, phosphoramide (Beaucage etal. (1993) Tetrahedron 49(10):1925); phosphorothioate (Mag et al. (1991)Nucleic Acids Res. 19:1437; and U.S. Pat. No. 5,644,048),phosphorodithioate (Briu et al. (1989) J. Am. Chem. Soc. 111:2321),O-methylphophoroamidite linkages (see Eckstein, Oligonucleotides andAnalogues: A Practical Approach, Oxford University Press (1992)), andpeptide nucleic acid backbones and linkages (see, Egholm (1992) J. Am.Chem. Soc. 114:1895). Other analog nucleic acids include those withpositively charged backbones (Denpcy et al. (1995) Proc. Natl. Acad.Sci. USA 92: 6097); non-ionic backbones (U.S. Pat. Nos. 5,386,023,5,637,684, 5,602,240, 5,216,141 and 4,469,863) and non-ribose backbones,including those described in U.S. Pat. Nos. 5,235,033 and 5,034,506.Nucleic acids containing one or more carbocyclic sugars are alsoincluded within the definition of nucleic acids (see Jenkins et al.(1995) Chem. Soc. Rev. pp. 169-176), and analogs are also described in,e.g., Rawls, C & E News Jun. 2, 1997 page 35. These modifications of theribose-phosphate backbone may be done to facilitate the addition ofadditional moieties such as labels, or to alter the stability andhalf-life of such molecules in physiological environments.

In addition to the naturally occurring heterocyclic bases that aretypically found in nucleic acids (e.g., adenine, guanine, thymine,cytosine, and uracil), nucleotide analogs also may include non-naturallyoccurring heterocyclic bases, such as those described in, e.g., Seela etal. (1999) Helv. Chim. Acta 82:1640. Certain bases used in nucleotideanalogs act as melting temperature (Tm) modifiers. For example, some ofthese include 7-deazapurines (e.g., 7-deazaguanine, 7-deazaadenine,etc.), pyrazolo[3,4-d]pyrimidines, propynyl-dN (e.g., propynyl-dU,propynyl-dC, etc.), and the like. See, e.g., U.S. Pat. No. 5,990,303,which is incorporated herein by reference. Other representativeheterocyclic bases include, e.g., hypoxanthine, inosine, xanthine; 8-azaderivatives of 2-aminopurine, 2,6-diaminopurine, 2-amino-6-chloropurine,hypoxanthine, inosine and xanthine; 7-deaza-8-aza derivatives ofadenine, guanine, 2-aminopurine, 2,6-diaminopurine,2-amino-6-chloropurine, hypoxanthine, inosine and xanthine;6-azacytidine; 5-fluorocytidine; 5-chlorocytidine; 5-iodocytidine;5-bromocytidine; 5-methylcytidine; 5-propynylcytidine;5-bromovinyluracil; 5-fluorouracil; 5-chlorouracil; 5-iodouracil;5-bromouracil; 5-trifluoromethyluracil; 5-methoxymethyluracil;5-ethynyluracil; 5-propynyluracil, and the like.

A “nucleoside” refers to a nucleic acid component that comprises a baseor basic group (comprising at least one homocyclic ring, at least oneheterocyclic ring, at least one aryl group, and/or the like) covalentlylinked to a sugar moiety (a ribose sugar or a deoxyribose sugar), aderivative of a sugar moiety, or a functional equivalent of a sugarmoiety (e.g. a carbocyclic ring). For example, when a nucleosideincludes a sugar moiety, the base is typically linked to a 1′-positionof that sugar moiety. As described above, a base can be a naturallyoccurring base or a non-naturally occurring base. Exemplary nucleosidesinclude ribonucleosides, deoxyribonucleosides, dideoxyribonucleosidesand carbocyclic nucleosides.

A “nucleotide” refers to an ester of a nucleoside, e.g., a phosphateester of a nucleoside, having one, two, three or more phosphate groupscovalently linked to a 5′ position of a sugar moiety of the nucleoside.

A “purine nucleotide” refers to a nucleotide that comprises a purinebase, whereas a “pyrimidine nucleotide” refers to a nucleotide thatcomprises a pyrimidine base.

An “oligonucleotide” refers to a nucleic acid polymer that includes atleast two, but typically 5-50 nucleotides and more typically, between 15and 35 nucleotides. The exact size of an oligonucleotide generallydepends on various factors, including the ultimate function or use ofthe oligonucleotide. Oligonucleotides may be prepared by any suitablemethod known in the art, including, for example, cloning and restrictiondigestion of appropriate sequences, or direct chemical synthesis by amethod such as the phosphotriester method of Narang et al. (1979) Meth.Enzymol. 68:90-99; the phosphodiester method of Brown et al. (1979)Meth. Enzymol. 68:109-151; the diethylphosphoramidite method of Beaucageet al. (1981) Tetrahedron Lett. 22:1859-1862; the triester method ofMatteucci et al. (1981) J. Am. Chem. Soc. 103:3185-3191; automatedsynthesis methods; the solid support method of U.S. Pat. No. 4,458,066or any other chemical method known in the art.

A “primer nucleic acid” or “primer” is an oligonucleotide that canhybridize to a template nucleic acid and permit chain extension orelongation using a nucleotide incorporating biocatalyst. Although otherprimer lengths are sometimes utilized, primers typically range from 15to 35 nucleotides. Short primer nucleic acids generally utilize coolertemperatures to form sufficiently stable hybrid complexes with templatenucleic acids. A primer nucleic acid that is at least partiallycomplementary to a subsequence of a template nucleic acid is typicallysufficient to hybridize with the template nucleic acid for extension tooccur. However, the success of the extension generally requires greatercomplementarity (i.e. fewer mismatches with the template) at the 3′-endof the primer. A primer nucleic acid can be labeled, if desired, byincorporating a label detectable by radiological, spectroscopic,photochemical, biochemical, immunochemical, or chemical techniques.

An “extended primer” refers to a primer to which one or more additionalnucleotides have been added. “Primer extension” is the action of theenzyme by which additional nucleotides are added to the primer.

A “template nucleic acid”, “template” or “target” refers to a nucleicacid to which a primer nucleic acid can hybridize and be extended undersuitable conditions. In the context of nucleic acid amplification,“target” is preferably a region of double stranded nucleic acid,consisting of the sequences at least partially complementary to at leasttwo primer sequences and the intervening sequence. A target can also bea single stranded nucleic acid, consisting of a sequence at leastpartially complementary to one primer and a sequence partially identicalto the second primer. Template nucleic acids can exist as isolatednucleic acid fragments or be a part of a larger nucleic acid fragment.Target nucleic acids can be derived or isolated from essentially anysource, such as cultured microorganisms, uncultured microorganisms,complex biological mixtures, tissues, sera, ancient or preserved tissuesor samples, environmental isolates or the like. Further, templatenucleic acids optionally include or are derived from cDNA, RNA, genomicDNA, cloned genomic DNA, genomic DNA libraries, enzymatically fragmentedDNA or RNA, chemically fragmented DNA or RNA, physically fragmented DNAor RNA, or the like. Template nucleic acids can also be chemicallysynthesized using techniques known in the art.

As used herein, a “gene” refers to any segment of DNA associated with abiological function. Thus, genes include coding sequences andoptionally, the regulatory sequences required for the expression of thecoding sequences.

Nucleic acids are “extended” or “elongated” when additional nucleotidesare incorporated into the nucleic acids, for example by a nucleotideincorporating biocatalyst, at the 3′ end of a nucleic acid.

A “moiety” or “group” refers to one of the portions into whichsomething, such as a molecule, is divided (e.g., a functional group,substituent group, or the like). For example, a nucleotide typicallycomprises a base group (e.g., adenine, thymine, cytosine, guanine,uracil, or an analog), a sugar moiety, and one or more phosphate groups.

An “alkyl group” refers to a linear, branched, or cyclic saturatedhydrocarbon moiety and includes all positional isomers, e.g., methyl,ethyl, propyl, butyl, 1-methylpropyl, 2-methylpropyl, 1,1-dimethylethyl,pentyl, 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, 2,2-dimethylpropyl,1-ethylpropyl, hexyl, 1,1-dimethylpropyl, 1,2-dimethylpropyl,1-methylpentyl, 2-methylpentyl, 3-methylpentyl, 4-methylpentyl,1,1-dimethylbutyl, 1,2-dimethylbutyl, 1,3-dimethylbutyl,2,2-dimethylbutyl, 2,3-dimethylbutyl, 3,3-dimethylbutyl, 1-ethylbutyl,2-ethylbutyl, 1,1,2-trimethylpropyl, 1,2,2-trimethylpropyl,1-ethyl-1-methylpropyl and 1-ethyl-2-methylpropyl, n-hexyl, cyclohexyl,n-heptyl, n-octyl, 2-ethylhexyl, n-nonyl, n-decyl and the like. An alkylgroup typically comprises about 1-20 carbon atoms and more typicallycomprises about 2-15 carbon atoms. Alkyl groups can be substituted orunsubstituted.

An “alkoxy group” refers to an alkyl group that comprises an oxygen atomand includes, e.g., methoxy, ethoxy, propoxy, butoxy, pentoxy,heptyloxy, octyloxy, and the like.

An “aryl group” refers to a substituent group of atoms or moiety that isderived from an aromatic compound. Exemplary aryl groups include, e.g.,phenyl groups, or the like. Aryl groups optionally include multiplearomatic rings (e.g., diphenyl groups, etc.). In addition, an aryl groupcan be substituted or unsubstituted.

An “aryloxy group” refers an aryl group that comprises an oxygen atomand includes, e.g., phenoxy, chlorophenoxy, methylphenoxy,methoxyphenoxy, butylphenoxy, pentylphenoxy, benzyloxy, and the like.

An “alkyl-aryl group” refers to a group that comprises alkyl and arylmoieties. Examples of the alkyl-aryl groups include benzyl groups, tolylgroups and xylyl groups.

An amplification assay is “selective” or “allele-selective” if it yieldsa predominance (i.e., a majority but less than 100%) of one product overother possible products. An assay is described as “allele-selective” aslong as amplification of the undesired (mismatched) variant of thetarget sequence is detectable. The term “specific” or “allele-specific”amplification assay is used if one of the possible products is formedexclusively. The assay where amplification of the undesired (mismatched)target is undetectable is called “allele-specific.” As the methods ofdetection become more sensitive, some assays previously known to beallele-specific, turn out to be allele-selective, i.e. someamplification of undesired variants of the target becomes detectable.Therefore, in the context of this invention, the term “allele-specific”is meant to encompass both strictly allele-specific, as well asallele-selective amplification.

A “genotype” refers to all or part of the genetic constitution of a cellor subject, or group of cells or subjects. For example, a genotypeincludes the particular mutations and/or alleles (e.g., polymorphisms,such as single nucleotide polymorphisms (SNPs) or the like) present at agiven locus or distributed in a genome.

A “nucleotide incorporating biocatalyst” or “nucleotide incorporatingenzyme” refers to a catalyst (or enzyme) that catalyzes theincorporation of nucleotides into a nucleic acid. Exemplary nucleotideincorporating enzymes include, DNA polymerases, RNA polymerases,terminal transferases, reverse transcriptases, telomerases and the like.

A “thermostable enzyme” refers to an enzyme that is stable (i.e.,resists breakdown or denaturation) and retains sufficient catalyticactivity when subjected to elevated temperatures for selected periods oftime. For example, a thermostable polymerase retains sufficient activityto effect subsequent primer extension reactions, when subjected toelevated temperatures for the time necessary to denature double-strandednucleic acids. Heating conditions necessary for nucleic aciddenaturation are well known in the art and are exemplified in U.S. Pat.Nos. 4,683,202 and 4,683,195. As used herein, a thermostable polymeraseis typically suitable for use in a temperature cycling reaction such asthe polymerase chain reaction (“PCR”). The examples of thermostablenucleic acid polymerases include Thermus aquaticus Taq DNA polymerase,Thermus sp. Z05 polymerase, Thermus flavus polymerase, Thermotogamaritima polymerases, such as TMA-25 and TMA-30 polymerases, Tth DNApolymerase, and the like.

A “modified” enzyme refers to an enzyme comprising an amino acid polymerin which at least one monomer differs from the reference sequence, suchas a native or wild-type form of the enzyme or another modified form ofthe enzyme. Exemplary modifications include monomer insertions,deletions, and substitutions. Modified enzymes also include chimericenzymes that have identifiable component sequences (e.g., structural orfunctional domains, etc.) derived from two or more parents. Alsoincluded within the definition of modified enzymes are those comprisingchemical modifications of the reference sequence. The examples ofmodified polymerases include G46E E678G CS5 DNA polymerase, G46E L329AE678G CS5 DNA polymerase, G46E L329A D640G S671F CS5 DNA polymerase,G46E L329A D640G S671F E678G CS5 DNA polymerase, a G46E E678G CS6 DNApolymerase, ΔZ05 polymerase, ΔZ05-Gold polymerase, ΔZ05R polymerase,E615G Taq DNA polymerase, E678G TMA-25 polymerase, E678G TMA-30polymerase, and the like.

The term “5′ to 3′ nuclease activity” or “5′-3′ nuclease activity”refers to an activity of a nucleic acid polymerase, typically associatedwith the nucleic acid strand synthesis, whereby nucleotides are removedfrom the 5′ end of nucleic acid strand, e.g., E. coli DNA polymerase Ihas this activity, whereas the Klenow fragment does not.

A polymerase that “substantially lacks 5′-3′ nuclease activity” refersto a polymerase that has 50% or less (e.g., <25%, <20%, <15%, <10%)5′-3′ nuclease activity than Taq DNA polymerase. Methods of measuring5′-3′ nuclease activity and conditions for measurement are well known inthe art. See, e.g., U.S. Pat. No. 5,466,591. Examples of DNA polymerasessubstantially lacking 5′ to 3′ nuclease activity include the Klenowfragment of E. coli DNA polymerase I; a Thermus aquaticus DNA polymerase(Taq) lacking the N-terminal 235 amino acids (e.g., as described in U.S.Pat. No. 5,616,494 and commonly referred to in the art as the “Stoffelfragment”). Other examples include a thermostable DNA polymerase havingsufficient deletions (e.g., N-terminal deletions), mutations, ormodifications so as to eliminate or inactivate the domain responsiblefor the 5′-3′ nuclease activity. See, e.g., U.S. Pat. No. 5,795,762.

A “label” refers to a moiety attached (covalently or non-covalently), toa molecule and capable of providing information about the molecule.Exemplary labels include fluorescent labels, colorimetric labels,chemiluminescent labels, bioluminescent labels, radioactive labels,mass-modifying groups, antibodies, antigens, biotin, haptens, andenzymes (including peroxidase, phosphatase, etc.).

A “hot start”, in the context of a nucleic acid amplification reaction,refers to a protocol, where at least one critical reagent is withheldfrom the reaction mixture (or, if present in the reaction mixture, thereagent remains inactive) until the temperature is raised sufficientlyto provide the necessary hybridization specificity of the primer orprimers. A “hot start enzyme” is an enzyme, typically a nucleic acidpolymerase, capable of acting as the “withheld” or inactive reagent in ahot start protocol.

A “Watson-Crick base pairing” or simply “base pairing” refers to“conventional” hydrogen bonding within a double-stranded nucleic acidmolecule. Watson-Crick base pairing is hyrdrogen bonding between adenineand thymine, between guanine and cytosine, between adenine and uracil,and between analogs of these bases.

The terms “scorpion” or “scorpion-like” denote unimolecular primer-probecombination as described in Whitcombe et al., (1999). Detection of PCRproducts using self-probing amplicons and fluorescence, Nature Biotech.17:804-807. Scorpion or scorpion-like primers within the meaning of thepresent invention incorporate the typical elements of the scorpion,namely a probe portion, a stem loop portion and a primer portion. Anexample of “scorpion” or “scorpion-like” unimolecular primer-probeformat is schematically illustrated in FIG. 7.

As mentioned above, in one aspect, the present invention relates to amethod of allele-specific amplification, comprising (a) providing asample, possibly containing at least one variant of a target sequence;(b) providing a first oligonucleotide, at least partially complementaryto more than one variant of the target sequence; (c) providing a secondoligonucleotide, at least partially complementary to one or morevariants of the target sequence, having a 3′-terminal nucleotidecomplementary to only one variant of the target sequence; wherein saidsecond oligonucleotide incorporates at least one nucleotide with a basecovalently modified at the exocyclic amino group; (d) providingconditions suitable for the hybridization of said first and secondoligonucleotides to at least one variant of the target sequence; (e)providing conditions suitable for the oligonucleotide extension by anucleotide incorporating biocatalyst; wherein said biocatalyst iscapable of extending said second oligonucleotide when it is hybridizedto the variant of the target sequence for which it has saidcomplementary 3′-terminal nucleotide, and substantially less when saidsecond oligonucleotide is hybridized to the variant of the targetsequence for which it has a non-complementary 3′-terminal nucleotide.

The second oligonucleotide, at least partially complementary to one ormore variants of the target sequence, having a 3′-terminal nucleotidecomplementary to only one variant of the target sequence is referred toas a “selective oligonucleotide,” “selective primer,” or“allele-selective primer.” The selective oligonucleotide of the presentinvention comprises 10-50, more preferably 15-35 nucleotides, themajority of them complementary to a sequence in more then one variant ofthe target sequence. The 3′-terminal nucleotide of the oligonucleotideis complementary to a variant of the target sequence, that is to beamplified and not complementary to other variants. The selectiveoligonucleotide of the present invention includes one or morenucleotides with a base, covalently modified at the exocyclic aminogroup. In some embodiments, the modified-base nucleotide occurs between1 and 5, but preferably 3 nucleotides upstream of the 3′-terminalnucleotide (also designated as −1, −2, −3, −4, −5 or N−1, N−2, N−3, N−4,N−5 positions herein). In other embodiments, the modified-basenucleotide is the 3′-terminal nucleotide. In some embodiments, themodified-base nucleotide occurs both at the 3′-terminus and at leastonce more, elsewhere within the oligonucleotide.

The allele-specific primer of the present invention may incorporatevarious aspects of primer design known in the art. For example, theprimer may take the form of a unimolecular primer-probe combinationtermed “scorpion” and described in Whitcombe et al., (1999) Detection ofPCR products using self-probing amplicons and fluorescence, NatureBiotech. 17:804-807. The scorpion primer designed according to thepresent invention incorporates the typical elements of the scorpion,namely a probe portion, a stem loop portion and a primer portion.Further, in a scorpion designed according to the present invention, theprimer portion has a 3′ end complementary to the variant position. Theprimer portion in a scorpion designed according to the present inventioncontains one or more chemically modified nucleotides as describedherein.

The nucleotides with covalent modifications of the exocyclic aminogroups have been described in U.S. Pat. No. 6,001,611, which isincorporated herein by reference. The synthesis of such nucleotides, andoligonucleotides incorporating such nucleotides are also described inthe '611 patent.

According to the present invention, a suitable modification of theexocyclic amino group may be selected based on the presence of thefollowing properties: (1) the modification interferes with but does notprevent Watson-Crick base pairing of the modified base with thecomplementary base in the double-stranded nucleic acid; (2) themodification interferes with but does not prevent the extension of theprimer containing the modified base by the nucleic acid polymerase; (3)the modification allows synthesis of the strand complementary to thestrand incorporating the modified base; and (4) the modificationincreases selectivity of a primer incorporating the modification.

The examples of exocyclic amino groups include the amino groups in the6-position of adenosine, 2-position of guanosine and 4-position ofcytidine. Exocyclic amino groups that take part in base pairing with thecomplementary nucleic acid strand may also occur in variousunconventional nitrogenous bases in nucleotides. Examples of nucleosideswith unconventional bases include, without limitation,3-methyladenosine, 7-methylguanosine, 3-methylguanosine,5-methylcytidine, and 5-hydroxymethylcytidine. Suitable modifications ofexocyclic amino groups of such unconventional bases may also be selectedaccording to the empirical method of the present invention.

The structures of the modified nucleotides containing a modifiedadenine, guanine, and cytosine base, respectively, are shown below,

where S represents the sugar moiety, and R represents the modifiergroup. A variety of modifier groups are envisioned which possess thefour properties outlined above. In certain embodiments, modifier groupshave the structure:

wherein R₁ and R₂ are independently selected from the group consistingof hydrogen, alkyl, alkoxy, unsubstituted or substituted aryl andphenoxy.

Alkyl groups may be branched or unbranched

Alkyl groups can be C₁-C₂₀ alkyls, for example C₁-C₁₀ alkyls.

Alkoxy groups can be C₁-C₂₀ alkoxy, for example C₁-C₁₀ alkoxy.

Aryl can be unsubstituted or substituted phenyl or naphtyl.

In one embodiment, R is a benzyl group or a substituted benzyl group. Incertain embodiments, substituted benzyl groups can have the followingstructure:

wherein R₃ represents a C₁-C₆ branched or unbranched alkyl group, morepreferably a C₁-C₄ branched or unbranched alkyl group, an alkoxy group,or a nitro group. Preferably, R₃ is attached in the para-position.

In some embodiments, the modifier groups are represented by structuresshown below:

In general, empirical selection of a particular suitable modifier groupfrom the class of compounds described herein can be carried outroutinely by one of skill in the art, based on the presence of the fourproperties listed above. Preferably, suitability of a particular groupis determined empirically by using the primers with modified nucleotidesin an allele-specific amplification reaction. The suitability of themodification is indicated by the increased selectivity of the reactionutilizing a primer with the base modification, when compared to anidentical reaction with an unmodified primer.

In some embodiments of the invention, the amplification involves thepolymerase chain reaction, i.e. repeated cycles of templatedenaturation, annealing (hybridization) of the oligonucleotide primer tothe template, and extension of the primer by thenucleotide-incorporating biocatalyst. In some embodiments, the annealingand extension occur at the same temperature step.

In some embodiments, the amplification reaction involves a hot startprotocol. In the context of allele-specific amplification, theselectivity of the allele-specific primers with respect to themismatched target may be enhanced by the use of a hot start protocol.Many hot start protocols are known in the art, for example, the use ofwax, separating the critical reagents from the rest of the reactionmixture (U.S. Pat. No. 5,411,876), the use of a nucleic acid polymerase,reversibly inactivated by an antibody (U.S. Pat. No. 5,338,671), anucleic acid polymerase reversibly inactivated by an oligonucleotidethat is designed to specifically bind its active site (U.S. Pat. No.5,840,867) or the use of a nucleic acid polymerase with reversiblechemical modifications, as described e.g. in U.S. Pat. Nos. 5,677,152and 5,773,528.

In some embodiments of the invention, the allele-specific amplificationassay is the real-time PCR assay. In a real-time PCR assay, the measureof amplification is the “cycles to threshold” or Ct value. An earlier Ctvalue reflect the rapid achievement of the threshold level and thus amore efficient amplification. The later Ct value may reflect inefficientor inhibited amplification. In the context of an allele-specificreal-time PCR assay, the difference in Ct values between the matched andthe mismatched templates is a measure of the discrimination between thealleles or the selectivity of the assay.

The allele-specific amplification assay may employ any suitablenucleotide-incorporating biocatalyst known in the art. For anallele-specific PCR assay, any thermostable nucleotide incorporatingbiocatalyst may be used. It is sometimes desirable to use an enzymewithout the proof-reading (3′-5′-exonuclease) activity, such as forexample, Taq DNA polymerase. It may also be desirable to use enzymes,substantially or entirely lacking the 5′-3′ nuclease activity, such asdescribed in U.S. Pat. No. 5,795,762. One example of such an enzyme isΔZ05 polymerase. It may sometimes be desirable to have an enzyme with a“hot start” capability, such as the reversibly modified enzymesdescribed in U.S. Pat. Nos. 5,677,152 and 5,773,528. One example of ahot-start enzyme is ΔZ05-Gold polymerase.

Detection of the amplification products may be accomplished by anymethod known in the art. These methods include the use of labeledprimers and probes as well as various nucleic acid-binding dyes. Themeans of detection may be specific to one variant of the targetsequence, or may be generic to all variants of the target sequence oreven to all double stranded DNA. The non-specific detection methods maybe used where the amplification of the undesired variants of the targetis minimal and expected to fall below the detection limit of the method.

The amplification products may be detected after the amplification hasbeen completed, for example, by gel electrophoresis of the unlabeledproducts and staining of the gel with a nucleic acid-binding dye.Alternatively, the amplification products may carry a radioactive or achemical label, either by virtue of incorporation during synthesis or byvirtue of being the extension products of a labeled primer. After, orduring electrophoresis, the labeled amplification products may bedetected with suitable radiological or chemical tools known in the art.After electrophoresis, the product may also be detected with atarget-specific probe labeled by any one of the methods known in theart. The labeled probe may also be applied to the target withoutelectrophoresis, i.e. in a “dot blot” assay or the like.

In other embodiments, the presence of the amplification product may bedetected in a homogeneous assay, i.e. an assay where the nascent productis detected during the cycles of amplification, or at least in the sameunopened tube, and no post-amplification handling is required. Ahomogeneous amplification assay has been described for example, in U.S.Pat. No. 5,210,015. Homogeneous amplification assay using nucleicacid-intercalating dyes has been described for example, in U.S. Pat.Nos. 5,871,908 and 6,569,627. The homogeneous assay may also employfluorescent probes labeled with two interacting fluorophores, such as“molecular beacon” probes (Tyagi et al., (1996) Nat. Biotechnol.,14:303-308) or fluorescently labeled nuclease probes (Livak et al.,(1995) PCR Meth. Appl., 4:357-362). In certain variations of thesetechnologies, an amplification product may also be identified by virtueof its distinctive melting temperature, see U.S. Pat. Nos. 5,871,908 and6,569,627. The amplification products may also be detected using aunimolecular primer-probe combination termed “scorpion.” Whitcombe etal., (1999) Detection of PCR products using self-probing amplicons andfluorescence, Nature Biotech. 17:804-807. The primer portion of thescorpion oligonucleotide may be an allele-specific primer designedaccording to the present invention.

In another aspect, the invention provides a reaction mixture forspecifically or selectively amplifying a selected variant of the targetsequence, comprising a first oligonucleotide, at least partiallycomplementary to more than one variant of the target sequence, a secondoligonucleotide, at least partially complementary to more than onevariant of the target sequence, but having a 3′-terminal nucleotidecomplementary to only one variant of the target sequence, wherein saidsecond oligonucleotide includes one or more nucleotides with a base,covalently modified at the exocyclic amino group, and a target nucleicacid, known to exist in more than one sequence variant. In someembodiments, the reaction mixture further comprises the reagents andsolutions generally necessary for the amplification of nucleic acids,including a nucleotide-incorporating biocatalyst, nucleic acidprecursors, i.e. nucleoside triphosphates, and organic and inorganicions, suitable for the support of the activity of thenucleotide-incorporating biocatalyst.

In another aspect, the invention provides kits for conductingallele-specific amplification according to the invention. The kitgenerally includes assay-specific components as well as componentsgenerally required for performing DNA amplification assays. As theassay-specific components, the allele-specific amplification kit of thepresent invention typically includes at least one allele-specificoligonucleotide, at least partially complementary to more than onevariant of the target sequence, having a 3′-terminal nucleotidecomplementary to only one variant of the target sequence and also havingone or more nucleotides with a base covalently modified at the exocyclicamino group, optionally, a second oligonucleotide, at least partiallycomplementary to more than one variant of the target sequence andoptionally a control nucleic acid sequence comprising an amount of atleast one variant of the control target sequence, at least partiallycomplementary to the oligonucleotides enclosed in the kit. In someembodiments, more than one variant of the control nucleic acid sequencemay be enclosed. In certain embodiments, among the several variants ofthe control nucleic acid sequence enclosed in the kit, at least onevariant is complementary to the 3′-terminal nucleotide of theallele-selective oligonucleotide. As the components generally requiredfor nucleic acid amplification, the kit of the present inventiontypically includes one or more of a nucleotide incorporatingbiocatalyst, nucleic acid precursors, such as nucleoside triphosphates(deoxyribonucleoside triphosphates or ribonucleoside triphosphates),optionally, a pyrophosphatase, for minimizing pyrophosphorolysis ofnucleic acids, a uracil N-glycosylase (UNG) for protection againstcarry-over contamination of amplification reactions, pre-made reagentsand buffers necessary for the amplification reaction and detection, anda set of instructions for conducting allele-specific amplification ofthe present invention.

In yet another aspect, the invention provides an oligonucleotide for usein allele-specific PCR. A typical oligonucleotide for use inallele-specific PCR of the present invention comprises 10-50, morepreferably 15-35 nucleotides, the majority of them complementary to asequence in more then one variant of the target sequence. However, the3′-terminal nucleotide of the oligonucleotide is complementary to onevariant of the target sequence and not complementary to other variants.Further, the oligonucleotide of the present invention includes one ormore nucleotides with a base covalently modified at the exocyclic aminogroup. In some embodiments, the modified-base nucleotide occurs between1 and 30, for example between 1 and 10, between 1 and 5, or for example1, 2 or 3 nucleotides upstream of the 3′-terminal nucleotide. In otherembodiments, the modified-base nucleotide is the 3′-terminal nucleotide.In some embodiments, the modified-base nucleotide occurs both at the3′-terminus as well as elsewhere within the oligonucleotide.

Without being bound by a particular theory, the inventors hypothesizethat the covalent base modifications of the present invention,especially the bulky groups, destabilize, but do not entirely disrupthydrogen bonding in the context of Watson-Crick base pairing between theprimer and the template nucleic acid. When the modification is combinedwith a non-complementary base at the same or nearby position within theprimer (as on the undesirable or “mismatched” variant of the targetsequence), the combined weakness of hydrogen bonding destabilizes theprimer-target nucleic acid complex to the extent that the extension ofthe oligonucleotide by the nucleotide-incorporating biocatalyst ispartially or completely inhibited. However, when the modification of thebase is present alone, without the non-complementary base (as on thedesirable or “matched” variant of the target sequence, which is to beamplified), the primer is extended efficiently. FIG. 1 is a diagramillustrating the position of the polymorphism and the primermodifications, and their role in allowing the amplification or thematched target but inhibiting the amplification of the mismatchedtarget.

The following examples and figures are provided to aid the understandingof the present invention, the true scope of which is set forth in theappended claims. It is understood that modifications can be made in theprocedures set forth without departing from the spirit of the invention.

EXAMPLES

The examples below utilize a “matched” and a “mismatched” target. Asused in the examples, the matched target is designed to be complementaryto the allele-specific amplification primer. The mismatched target isdesigned to have a mismatch with the 3′-terminal nucleotide of theallele-specific primer.

As a matched target, the examples utilize the V600E mutation of thehuman BRAF gene. This mutation is a valine-to-glutamate change of aminoacid 600, that results from a thymine (T) to adenine (A) transition atnucleotide 1799 of the BRAF gene. The mutation is found in many cancersand is thought to contribute to cancer progression, as it results inconstitutive activation of the MAPK pathway. Detection of this singlenucleotide change in a population of tumor cells has utility in thediagnosis and treatment of human cancers.

The mutant target is “matched”, i.e. forms an A-T Watson-Crick pair withthe 3′-terminal nucleotide of each of the allele-specific primers (Table1). The mismatched target is the wild-type BRAF sequence. The mismatchedtarget forms an A-A mismatch with the 3′-terminal nucleotide of theallele-specific primers.

TABLE 1  Primers and probes Allele-specific primers SEQ ID5′-AGTAAAAATAGGTGATTTTGGTCTAGCTACAGA-3′ NO: 3 SEQ ID5′-AGTAAAAATAGGTGATTTTGGTCTAGCTACXGA-3′ NO: 4 SEQ ID5′-AGTAAAAATAGGTGATTTTGGTCTAGCTACYGA-3′ NO: 5 SEQ ID5′-AGTAAAAATAGGTGATTTTGGTCTAGCTACAGY-3′ NO: 7 SEQ ID5′-AGTAAAAATAGGTGATTTTGGTCTAGCTYCAGY-3′ NO: 8 SEQ ID5′-AGTAAAAATAGGTGATTTTGGTCTAGCTACAGX-3′ NO: 10 SEQ ID5′-TAAAAATAGGTGATTTTGGTCTAGCTXCAGX-3′ NO: 11 Other primers and probesSEQ ID 5′-TAGCCTCAATTCTTACCATCCACAX-3′ NO: 6 SEQ ID5′-FTCGATGGAGTQGGGTCCCATCAGTTTGAACA- NOS 9 GTTGTCTp-3′ and 16X-N⁶-benzyl-dA Y-N⁶-para-tert-butyl-benzyl-dA F-cx-FAM donor fluorophoreQ-BHQ-2 “Black Hole” quencher p-3′-phosphate The 3′-terminal nucleotidecorresponds to the variable position in the target

Example 1 Allele-Specific Amplification Using Primers with Internal BaseModifications

In this example, two variants of the template sequence were present inequal amounts, a matched variant, complementary to the primer sequenceand a mismatched variant. The matched variant was a plasmid DNA with theinsert incorporating the BRAF V600E mutant sequence (SEQ ID NO: 1),while the mismatched variant was the same plasmid with the BRAFwild-type sequence (SEQ ID NO: 2).

(BRAF V600E mutant sequence fragment): SED ID NO: 1 5′-AGTAAAAATAGGTGATTTTGGTCTAGCTACAGAGAAATCTCGATGGAGTGGGTCCCATCAGTTTGAACAGTTGTCTGGATCCATTTTGTGGATGG TAAGAATTGAGGCTA-3′(BRAF wild-type sequence fragment): SEQ ID NO: 2 5′-AGTAAAAATAGGTGATTTTGGTCTAGCTACAGTGAAATCTCGATGGAGTGGGTCCCATCAGTTTGAACAGTTGTCTGGATCCATTTTGTGGATGG TAAGAATTGAGGCTA-3′

The forward primers (SEQ ID NO: 3, 4, 5) and the reverse primer (SEQ IDNO: 6) are shown in Table 1. The primers contained an internalN⁶-benzyl-dA or an internal N⁶-para-tert-butyl-benzyl-dA whereindicated.

Each 100 μL reaction contained 10⁶ copies of either target, 5% glycerol,50 mM tricine (pH 8.3), 25 mM potassium acetate (pH 7.5), 200 μM eachdATP, dCTP and dGTP, 400 μM dUTP, 0.1 μM or one of the forward primers(SEQ ID NO: 3, 4 or 5), 0.7 μM reverse primer (SEQ ID NO: 6), 2 μMSyto-13 intercalating dye, 1% DMSO, 4 units uracil-N-glycosylase (UNG),10 units ΔZ05 polymerase, and 4 mM magnesium acetate.

Amplification and analysis were done using the Roche LightCycler 480instrument. The reactions were subjected to the following temperatureprofile: 50° C. for 5 minutes (UNG step), 95° C. for 10 minutes,followed by 80 cycles of 95° C. for 15 seconds and 59° C. for 40seconds. Fluorescence data was collected at the end of each 59° C. step.

The results are shown on FIG. 2. The amplification results are expressedas a change in fluorescence in the 450-500 nm wavelength interval. Theselectivity of the amplification is measured by the difference in the Ctvalue (ΔCt) between the matched and the mismatched targets. ΔCt for eachexperiment is indicated on FIG. 2. The data shows that the matched(mutant) variant of the target was amplified selectively over themismatched (wild-type) variant. The selectivity was enhanced by the basemodification of the nucleotides in the primers.

Example 2 Allele-Specific Amplification Using Primers with One or MoreInternal and 3′-Terminal Base Modifications

For this experiment, the same matched (mutant) and mismatched(wild-type) targets as in Example 1 were used. The primers containedbase modifications at an internal position, 3′-terminal position orboth.

Each 100 μL reaction contained 10⁶ copies of either target, 5% glycerol,50 mM tricine (pH 8.3), 90 mM potassium acetate (pH 7.5), 200 μM eachdATP, dCTP and dGTP, 400 μM dUTP, 0.5 μM of one of the forward primers(SEQ ID NO: 3, 5, 7 or 8), 0.5 μM reverse primer (SEQ ID NO: 6), 0.2 μMfluorogenic probe (SEQ ID NOS 9 and 16), 1% DMSO, 4 unitsuracil-N-glycosylase (UNG), 10 units Z05 polymerase, and 5 mM magnesiumacetate.

Amplification and analysis were done using the Roche LightCycler 480instrument. Reactions were subjected to the following temperatureprofile: 50° C. for 5 minutes (UNG step), 95° C. for 10 minutes,followed by 60 cycles of 95° C. for 15 seconds and 59° C. for 40seconds. Fluorescence data was collected at the end of each 59° C. step.

The results are shown on FIG. 3 in the same format as the results of theExample 1, except the fluorescence is measured in the 483-553 nmwavelength interval. The data demonstrates that the base modificationsof the primer improve the selectivity of the amplification assay, andseveral modified bases may have a cumulative effect on selectivity.

Example 3 Allele-Specific Amplification Using a Primer with a BaseModification and Various DNA Polymerases

In this example, the same matched (mutant) and mismatched (wild-type)targets as in Example 1, where amplified using a primer with a singleinternal base modification. The amplification was carried out in thepresence of Z05, ΔZ05, or ΔZ05-Gold polymerase.

The Z05 reactions contained 10⁶ copies of template, 5% glycerol, 50 mMtricine (pH 8.3), 90 mM potassium acetate (pH 7.5), 200 μM each dATP,dCTP, and dGTP, 400 μM dUTP, 0.5 μM forward primer (SEQ ID NO: 5), 0.5μM reverse primer (SEQ ID NO: 6), 2 μM Syto-13 intercalating dye, 1%DMSO, 4 units uracil-N-glycosylase (UNG), 10 units of Z05 polymerase,and 5 mM magnesium acetate in 100 μL.

The ΔZ05 reactions contained 10⁶ copies of template, 5% glycerol, 50 mMtricine (pH 8.3), 25 mM potassium acetate (pH 7.5), 200 μM each dATP,dCTP and dGTP, 400 μM dUTP, 0.1 μM forward primer (SEQ ID NO: 5), 0.7 μMreverse primer (SEQ ID NO: 6), 2 μM Syto-13 intercalating dye, 1% DMSO,4 units uracil-N-glycosylase (UNG), 10 units ΔZ05 polymerase, and 4 mMmagnesium acetate in 100 μL.

The ΔZ05-Gold reactions contained 10⁶ copies of template, 8% glycerol,50 mM tricine (pH7.7), 45 mM potassium acetate (pH 7.5), 200 μM eachdATP, dCTP and dGTP, 400 μM dUTP, 0.1 μM forward primer (SEQ ID NO: 5),0.7 μM reverse primer (SEQ ID NO: 6), 2 μM Syto-13 intercalating dye, 1%DMSO, 2 units uracil-N-glycosylase (UNG), 60 units ΔZ05-Gold polymerase,and 3 mM magnesium acetate in 100 μL.

The results are shown on FIG. 4 in the same format as the results of theExample 2. The data demonstrates the relative ability of each enzyme toperform allele-selective amplification using base-modified primers.

Example 4 Allele-Specific Amplification Using Base-Modified Primers inthe Presence of Excess Amounts of Mismatched Template

In this example, the same matched (mutant) and mismatched (wild-type)targets as in Example 1 were used. The targets were amplified using aprimer with a single internal alkyl modification. To simulate clinicalsamples, the reactions contained an extremely low copy number of themutant (matched) target alone or in the presence of large excess of thewild-type (mismatched) target. In a separate reaction, a large amount ofthe mismatched target was present without any matched target.

The 100 μL reactions contained the indicated amount of target DNA, 8%glycerol, 50 mM tricine (pH7.7), 45 mM potassium acetate (pH 7.5), 200μM each dATP, dCTP and dGTP, 400 μM dUTP, 0.1 μM forward primer (SEQ IDNO: 5), 0.7 μM reverse primer (SEQ ID NO: 6), 0.2 μM fluorogenic probe(SEQ ID NOS 9 and 16), 1% DMSO, 2 units uracil-N-glycosylase (UNG), 60units ΔZ05-Gold polymerase, and 3 mM magnesium acetate.

The results are shown in FIG. 5 in the same format as the results of theExample 2. The data demonstrates that under the exemplary conditions,amplification is specific to the matched target, regardless of thepresence or relative amount of the mismatched target.

Example 5 Allele-Specific Amplification Using Scorpion ARMS-Like Primerswith Internal Base Modifications

TABLE 3  SEQ ID NO FUNCTION PRIMER SEQUENCE  3 FORWARD5′-AGTAAAAATAGGTGATTTTGGTCTAGCTAC PRIMER AGA-3′ 12 FORWARD5′-FCCCGCGCGGACCCACTCCATCGAGAGCGC and 17 PRIMER,GGGQJAGTAAAAATAGGTGATTTTGGTCTAGCT PROBE ACAGA-3′  5 FORWARD5′-AGTAAAAATAGGTGATTTTGGTCTAGCTAC PRIMER YGA-3′ 13 FORWARD5′-FCCCGCGCGGACCCACTCCATCGAGAGCGC and 18 PRIMER,GGGQJAGTAAAAATAGGTGATTTTGGTCTAGCT PROBE ACYGA-3′ 14 REVERSE5′-TAGCCTCAATTCTTACCATCCACAX-3′ PRIMER 15 PROBE5′-FTCTCGATGGAGTGGGTCCQp-3′ X-N⁶-benzyl-dAY-N⁶-para-tert-butyl-benzyl-dA F-cx-FAM donor fluorophore Q-BHQ-2 “BlackHole” quencher J-HEG p-3′-phosphate * The allele selective nucleotide isunderlined (N or N-1 position from 3′ terminus)

In this example, two variants of the template sequence were present inequal amounts, a matched variant, complementary to the primer sequenceand a mismatched variant. The matched variant was a plasmid DNA with theinsert representing the BRAF V600E mutant sequence (SEQ ID NO: 1), whilethe mismatched variant was the same plasmid with the BRAF wild-typesequence (SEQ ID NO: 2). The forward primers (SEQ ID NO: 3, 5, 12, 13,17 and 18) and reverse primer (SEQ ID NO: 14) are as described in Table3. The forward, ASPCR primers, were designed with the SNP at the 3′terminal position, either with or without N6-tert-butyl-benzyl-dAmodification. The ASPCR primer is paired with a downstream detectionprobe (SEQ ID NO: 15) or linked to the probe complement in a closedScorpion-like format.

Each 50 uL reaction contained 10⁵ copies of either target, 5% glycerol,50 mM tricine (pH 8.3), 150 mM potassium acetate (pH 7.5), 200 μM eachof dATP, dCTP and dGTP, 400 μM dUTP, 0.4 μM forward primer, 0.4 μMreverse primer, 1% DMSO, 2 units uracil-N-glycosylase (UNG), 10 unitsZ05 polymerase, and 3 mM magnesium acetate. 0.2 uM of detection probewas added to reactions containing Primers 3 and 5 where the probecomplement is not linked to the forward primer.

Amplification and analysis were done using the Roche LightCycler 480instrument. The reactions were subjected to the following temperatureprofile: 50° C. for 5 minutes (UNG step) followed by 95 cycles of 95° C.for 15 seconds and 59° C. for 40 seconds. Fluorescence data wascollected at the 495-525 nm range at the end of each 59° C.anneal/extend step.

The results are shown on FIG. 6 and Table 4. The selectivity of theamplification is measured by the difference in the Ct value (ΔCt)between the matched and the mismatched targets. ΔCt for each experimentis indicated on each diagram and summarized in Table 4. The data showsthat the matched (mutant) variant of the target was amplifiedselectively over the mismatched (wild-type) variant using either theindividual primer and probe or the primer and probe linked in a closedScorpion-like format.

TABLE 4 POSITION OF MODIFICATION SEQ SELECTIVE PRIMER OF PRIMING WT MUTID NO PRIMER SEQUENCE NUCLEOTIDE FORMAT SEGMENT CTAVG CTAVG ΔCT  3AGTAAAAATAGGTGATTTTGGTCTA 3′ terminus Traditional none 31.6 30.2 1.4GCTACAGA 12 and FCCCGCGCGGACCCACTCCATCGAG 3′ terminus Scorpion none 34.729.2 5.5 17 AGCGCGGGQJAGTAAAAATAGGTGA ARMS TTTTGGTCTAGCTACAGA  5AGTAAAAATAGGTGATTTTGGTCTA 3′ terminus Traditional Y at N-2 38.1 29.5 8.6GCTACYGA 13 and FCCCGCGCGGACCCACTCCATCGAG 3′ terminus Scorpion Y at N-251.4 32.6 18.8 18 AGCGCGGGQJAGTAAAAATAGGTGA ARMS TTTTGGTCTAGCTACYGA

While the invention has been described in detail with reference tospecific examples, it will be apparent to one skilled in the art thatvarious modifications can be made within the scope of this invention.Thus the scope of the invention should not be limited by any of theexamples described herein, but by the claims presented below. Allpublications including patent applications and patents cited in thisapplication are incorporated by reference in their entirety for allpurposes to the same extent as if each individual publications wereindividually indicated to be incorporated by reference for all purposes.

The invention claimed is:
 1. A kit for allele-specific amplification ofa target sequence, which exists in the form of several variantsequences, comprising (a) a first oligonucleotide, at least partiallycomplementary to one or more variant of the target sequence; and (b) asecond oligonucleotide, at least partially complementary to one or morevariant of the target sequence and having a 3′-terminal nucleotidecomplementary to only one variant of the target sequence; wherein saidsecond oligonucleotide is selected from a group consisting of SEQ IDNOs: 4, 5, 7, 8, 10, 11, and
 18. 2. An oligonucleotide for performing anallele-specific amplification of a target sequence, which exists in theform of several variant sequences, comprising a sequence at leastpartially complementary to a portion of one or more variants of saidtarget sequence; a 3′-terminal nucleotide which is complementary to onlyone variant of said target sequence and at least one nucleotide with abase covalently modified at the exocyclic amino group with a sequenceselected from a group consisting of SEQ ID NOs: 4, 5, 7, 8, 10, 11 and18.